The semaglutide impurity endo-17a-Ala-SMT is a structurally related impurity that may be produced during the synthesis or degradation of semaglutide (a glucagon-like peptide-1 (GLP-1) receptor agonist used to treat type 2 diabetes and obesity). This impurity is formed by modification of alanine (Ala), and its presence may affect the purity, stability and pharmacological activity of the drug. During the drug production process, strict quality control methods such as high-performance liquid chromatography (HPLC) or mass spectrometry analysis are required to monitor and control the content of such impurities to ensure that the safety and efficacy of the drug meet the pharmacopoeia standards and regulatory requirements.
Product Overview
Basic Description |
Structure and function: |
Three-letter sequence |
H-His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Lys-Glu-Ile-Trp-Leu-Val-Lys-Gly-Asp-Val-Arg-Arg-Arg-Arg-Arg-Arg-Gly-CONH2 |
Single letter sequence |
HHAEGTFTSDVSSYLEGQAKEITWLVLVKGDVRRAARRRRG-NH2 |
Molecular formula |
C187H290N54O59S |
Molecular weight |
4106.14 g/mol |
Product Attributes
purity |
>98% |
form |
Lyophilized powder |
Storage conditions |
Store at -20°C/-80°C away from light |